A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461409



Internal ID21118962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124204462..124209097hg38UCSC Ensembl
chr11:124075169..124079804hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg384636
hg194636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987793
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461409
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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